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Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina
Few prospective studies have documented the seropositivity among those children infected with severe acute respiratory syndrome coronavirus 2. From 2 April 2021 to 24 June 2021, we prospectively enrolled children between the ages of 2 and 17 years at three North Carolina healthcare systems. Particip...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154644/ https://www.ncbi.nlm.nih.gov/pubmed/37009915 http://dx.doi.org/10.1017/S0950268823000481 |
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author | Ahmed, Amina DeWitt, Michael E. Dantuluri, Keerti L. Castri, Paola Buahin, Asare LaGarde, William H. Weintraub, William S. Rossman, Whitney Santos, Roberto P. Gibbs, Michael Uschner, Diane |
author_facet | Ahmed, Amina DeWitt, Michael E. Dantuluri, Keerti L. Castri, Paola Buahin, Asare LaGarde, William H. Weintraub, William S. Rossman, Whitney Santos, Roberto P. Gibbs, Michael Uschner, Diane |
author_sort | Ahmed, Amina |
collection | PubMed |
description | Few prospective studies have documented the seropositivity among those children infected with severe acute respiratory syndrome coronavirus 2. From 2 April 2021 to 24 June 2021, we prospectively enrolled children between the ages of 2 and 17 years at three North Carolina healthcare systems. Participants received at least four at-home serological tests detecting the presence of antibodies against, but not differentiating between, the nucleocapsid or spike antigen. A total of 1,058 participants were enrolled in the study, completing 2,709 tests between 1 May 2021 and 31 October 2021. Using multilevel regression with poststratification techniques and considering our assay sensitivity and sensitivity, we estimated that the seroprevalence of infection-induced antibodies among unvaccinated children and adolescents aged 2–17 years in North Carolina increased from 15.2% (95% credible interval, CrI 9.0–22.0) in May 2021 to 54.1% (95% CrI 46.7–61.1) by October 2021, indicating an average infection-to-reported-case ratio of 5. A rapid rise in seropositivity was most pronounced in those unvaccinated children aged 12–17 years, based on our estimates. This study underlines the utility of serial, serological testing to inform a broader understanding of the regional immune landscape and spread of infection. |
format | Online Article Text |
id | pubmed-10154644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101546442023-05-03 Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina Ahmed, Amina DeWitt, Michael E. Dantuluri, Keerti L. Castri, Paola Buahin, Asare LaGarde, William H. Weintraub, William S. Rossman, Whitney Santos, Roberto P. Gibbs, Michael Uschner, Diane Epidemiol Infect Original Paper Few prospective studies have documented the seropositivity among those children infected with severe acute respiratory syndrome coronavirus 2. From 2 April 2021 to 24 June 2021, we prospectively enrolled children between the ages of 2 and 17 years at three North Carolina healthcare systems. Participants received at least four at-home serological tests detecting the presence of antibodies against, but not differentiating between, the nucleocapsid or spike antigen. A total of 1,058 participants were enrolled in the study, completing 2,709 tests between 1 May 2021 and 31 October 2021. Using multilevel regression with poststratification techniques and considering our assay sensitivity and sensitivity, we estimated that the seroprevalence of infection-induced antibodies among unvaccinated children and adolescents aged 2–17 years in North Carolina increased from 15.2% (95% credible interval, CrI 9.0–22.0) in May 2021 to 54.1% (95% CrI 46.7–61.1) by October 2021, indicating an average infection-to-reported-case ratio of 5. A rapid rise in seropositivity was most pronounced in those unvaccinated children aged 12–17 years, based on our estimates. This study underlines the utility of serial, serological testing to inform a broader understanding of the regional immune landscape and spread of infection. Cambridge University Press 2023-04-03 /pmc/articles/PMC10154644/ /pubmed/37009915 http://dx.doi.org/10.1017/S0950268823000481 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited. |
spellingShingle | Original Paper Ahmed, Amina DeWitt, Michael E. Dantuluri, Keerti L. Castri, Paola Buahin, Asare LaGarde, William H. Weintraub, William S. Rossman, Whitney Santos, Roberto P. Gibbs, Michael Uschner, Diane Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina |
title | Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina |
title_full | Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina |
title_fullStr | Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina |
title_full_unstemmed | Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina |
title_short | Characterisation of infection-induced SARS-CoV-2 seroprevalence amongst children and adolescents in North Carolina |
title_sort | characterisation of infection-induced sars-cov-2 seroprevalence amongst children and adolescents in north carolina |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154644/ https://www.ncbi.nlm.nih.gov/pubmed/37009915 http://dx.doi.org/10.1017/S0950268823000481 |
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